Aims & Objectives

  1. To provide a means by which people living with and/or affected by HIV, Hepatitis C, and Tuberculosis have a voice.
  2. To empower people living with, and/or affected by HIV, Hepatitis C, and Tuberculosis to access information and resources they need to improve the social and economic welfare of their communities.
  3. To campaign and advocate for the interests of people living with and/or affected by HIV, Hepatitis C and Tuberculosis, challenging that which adversely affects their welfare.
  4. To work in partnership with other stakeholders to influence governmental policy in such areas as human, civil and disability rights, immigration & migration, access to health care, treatments, standards of care, and social policy.
  5. To promote user involvement at all levels in the development of public policy and the planning, delivery and monitoring of services.
  6. To influence the regulatory authorities, the pharmaceutical industry and medical treatment system, on such issues, as biotechnology, drug trials, drug development, drugs access, pricing, etc.
  7. To encourage and assist in the development of local & national groups of positive people.
  8. To strengthen and further develop the Coalition to enable it to achieve its mission.

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The Patient can be as knowledgeable as the expert, but is uniquely placed to have a holistic view of their condition

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